At Hays, we are partnering with a leading Japanese pharmaceutical company that specializes in the manufacture and marketing of generic drugs and OTC products, with a significant presence in Spain.

We are currently seeking a
Medical Writer – Clinical Development.

What you will do
- Preparation of CSRs and interaction with the CRO.
- Review of clinical studies and reports 7-8. Clinical and bioanalytical review.
- Review of protocols.

What we are looking for
- +4 years of experience as a Medical Writer within the pharmaceutical, biotech, CRO, or life sciences industry.
- Proven experience in both clinical development and, ideally, bioanalytical studies.
- Strong expertise in the preparation, review, and quality control of clinical and regulatory documents.
- Comprehensive knowledge of ICH-GCP (Good Clinical Practice) guidelines and principles.
- Strong understanding of GLP (Good Laboratory Practice) requirements.
- Excellent scientific writing, editing, and proofreading skills.




- Ability to critically analyze and interpret complex clinical and scientific data.
- Strong attention to detail and commitment to document quality and compliance.
- Experience collaborating with cross-functional teams, including Clinical Operations, Biostatistics, Data Management, Regulatory Affairs, and Medical Affairs.
- Ability to manage multiple projects simultaneously while meeting tight timelines.
- English fluent.

What We Offer
- Commercial contract with Hays.
- Remote work option. Offices in Barcelona.
- Adaptable hours from 7:00 AM to 8:00 PM. 40 hours per week.
- The candidate must be a freelancer, registered as self-employed, and have liability insurance.
- International project.

? If you are interested in working in an international environment, we would love to hear from you.

📌 FREELANCE_ Medical Writer- REMOTE/ENGLISH (Barcelona)
🏢 Hays
📍 Barcelona